KR20210110327A - Adhesive composition comprising styrenic block copolymer and article containing same - Google Patents

Abstract

An adhesive composition is provided comprising a styrenic block copolymer and at least one tackifier, wherein the at least one tackifier contains a non-carbon heteroatom functional group, the adhesive composition comprising: It is washable and durable when bonded to Also provided are articles made using these adhesives.

Description

Adhesive composition comprising styrenic block copolymer and article containing same

Disclosed herein is an adhesive composition comprising a styrenic block copolymer and at least one tackifier containing non-carbon heteroatom functional groups. The adhesive composition is washable when bonded to a substrate.

The retroreflective material or article improves wearer visibility by returning incident light back towards the light source, which promotes safety for both professional workers (eg, traffic workers) and consumers (eg, drivers). Traditional binder materials for retroreflective materials involve solvent-based or water-based coating chemistries, where a binder solution is coated on top of an optical element layer. The resulting coating is laminated to fabric to create a fabric article, or laminated to a transfer adhesive to make a transfer article. Improvements are needed for retroreflective materials or articles that are durable to wash and maintain a good appearance after 25 wash cycles using the ISO 6330 Method 6N test protocol.

The present invention provides adhesive compositions useful for binder layers such that retroreflective materials or articles made using these adhesive compositions are durable to wash and have a good appearance after 25 wash cycles using the ISO 6330 Method 6N test protocol. will keep Also disclosed is an article comprising at least one binder layer and a layer of optical elements partially embedded within the at least one binder layer, wherein at least one of the binder layers comprises the disclosed adhesive composition.

In one aspect, the present invention provides an adhesive composition comprising a styrenic block copolymer and at least one tackifier, wherein the at least one tackifier contains a non-carbon heteroatom functional group, the adhesive composition comprising: It is wash-durable when bonded to a substrate. In some embodiments, the at least one tackifier containing a non-carbon heteroatom functional group has an acid number of at least 1 mg KOH/g.

In some embodiments, the adhesive composition is a laminating adhesive. In some embodiments, the adhesive composition is a heat activated adhesive. In some embodiments, the polarity index of the tackifier is at least 2.5. In some embodiments, the composition has a polarity index of 2.5 to 15.

In some embodiments, the styrenic block copolymer comprises styrenic end blocks and isoprene midblocks. In some embodiments, the styrenic block copolymer comprises diblocks of styrenic blocks and isoprene blocks.

In some embodiments, the total weight percent of all tackifiers in the adhesive composition is at least 5 weight percent, based on the total weight of the adhesive composition. In some embodiments, the adhesive composition further comprises at least 0.1% by weight of an antioxidant based on the total weight of the adhesive composition.

In another aspect, the present invention provides an article comprising any of the aforementioned adhesive compositions adhered to a laminating substrate. In some embodiments, the laminating substrate is selected from at least one of a layer of another adhesive, a film layer, a fabric layer, or a non-woven layer. In some embodiments, the disclosed articles further comprise a retroreflective applique disposed on the side of the adhesive composition opposite the laminating substrate. In some embodiments, the retroreflective applique is disposed on the article of clothing.

The above summary of the invention is not intended to describe each disclosed embodiment or every implementation of the invention. The following description more particularly exemplifies exemplary embodiments. In various places throughout this application, guidance is provided through lists of examples; Examples can be used in various combinations. In each case, the recited list serves only as a representative group and should not be construed as an exclusive list.

1 depicts a cross-sectional view of one embodiment of an article of clothing comprising the disclosed adhesive composition.
2 shows a cross-sectional view of one embodiment of an intermediate article of the present invention.
3 shows a cross-sectional view of one embodiment of an intermediate article of the present invention.
4 shows a cross-sectional view of one embodiment of an article of the present invention.
5 shows a cross-sectional view of one embodiment of an article of the present invention.
6 shows a top view of one embodiment of an article of the present invention.
7 shows an image after washing of fabrics to which various disclosed embodiments are adhered.
The drawings are not necessarily drawn to scale. Like reference numbers used in the drawings refer to like elements. It will be understood, however, that the use of a reference number to refer to a component in a given figure is not intended to limit that component in other figures labeled with the same reference number.

All scientific and technical terms used herein have their meanings commonly used in the art unless otherwise specified. The definitions provided herein are intended to facilitate understanding of certain terms frequently used herein, and are not intended to limit the scope of the present invention.

As used in this specification and the appended claims, the singular forms include embodiments with plural referents unless the content clearly dictates otherwise.

As used in this specification and the appended claims, the term "or" is generally used in its meaning including "and/or" unless the content clearly dictates otherwise. The term “and/or” means one or all of the listed elements, or a combination of any two or more of the listed elements.

As used herein, "has", "having", "contains", "comprising", "includes", "comprising", etc. are used in their open-ended sense, and are generally used in their open sense, such as "comprising but having means "not limited". It will be understood that "consisting essentially of," "consisting of," and the like are encompassed by "comprising" and the like.

As used herein, “consisting essentially of,” when it relates to a composition, device, system, method, etc., includes the listed components of the composition, device, system, method, etc., and the composition. , means limited to any other component that does not materially affect the basic and novel feature(s) of the apparatus, system, method, etc.

The words “preferred” and “preferably” refer to embodiments that may provide certain benefits under certain circumstances. However, under the same or other circumstances, other embodiments may also be desirable. Furthermore, the recitation of one or more preferred embodiments does not imply that other embodiments are not useful, nor is it intended to exclude other embodiments from the scope of the invention, including the claims.

Also, as used herein, recitation of a numerical range by an endpoint includes all numbers subsumed within that range (eg, 1 to 5 is 1, 1.5, 2, 2.75, 3, 3.80, 4, 5, etc., or 10 or less includes 10, 9.4, 7.6, 5, 4.3, 2.9, 1.62, 0.3, etc.). When a range of values is “below” a particular value, that value is included within that range.

Disclosed herein are retroreflective articles, and methods of making and using the same. In some embodiments, the retroreflective article comprises a rubber elastomeric binder layer, and a layer of optical elements partially embedded within the binder layer. In some embodiments, the retroreflective article includes a binder layer, a layer of optical elements partially embedded within the binder layer, and an additional application layer. The optical elements include transparent microspheres and at least one reflective layer. Optionally, the optical elements include one or more polymer intervening layers. Such intervening layers can provide any desired function. In some embodiments, it may serve as a physical protective layer and/or a chemical protective layer (eg, providing improved abrasion resistance, corrosion resistance, etc.). In some embodiments, such a layer may serve as a bonding layer (eg, a tie layer or adhesion-promoting layer) that may be bonded by a reflective layer as discussed later herein. It will be appreciated that some intervening layers may serve more than one, eg, all, of these purposes. In some embodiments, such an intervening layer may be transparent (specifically, it may be at least essentially free of any colorants, etc.). Organic polymer layers (eg, protective layers) and potentially suitable compositions thereof are described in detail in US Patent Application Publication No. 2017/0276844 (McCoy), which is incorporated herein by reference in its entirety. In certain embodiments, such a layer may be comprised of a polyurethane material. Various polyurethane materials that may be suitable for such purposes are described, for example, in US Patent Application Publication No. 2017/0131444 (Ying), which is incorporated herein by reference in its entirety. In some embodiments, the at least one tackifier in the rubber elastomeric binder layer further comprises a non-carbon heteroatom functional group. In some embodiments, the rubber elastomeric binder layer comprises a styrenic block copolymer. In some embodiments, the additional application layer comprises a rubber elastomer. In some embodiments, the disclosed retroreflective articles are wash durable when applied to a substrate.

An article of clothing is also disclosed herein. Referring to FIG. 1 , in some embodiments, an article of clothing has an adhesive composition having a first major surface attached to a first laminating substrate 15 and a second major surface attached to a second laminating substrate 17 (or application layer) ( 50 ). The first and second laminating substrates 15 , 17 may be layers of other adhesives, film layers, fabric layers, or nonwoven layers. The first and second laminating substrates 15 , 17 may be the same or different materials. In some embodiments, the adhesive composition (or application layer) 50 between the first laminating substrate 15 and the second laminating substrate 17 is a rubber elastomer comprising a styrenic block copolymer and a non-carbon heteroatom at least one tackifier having a functional group.

Also disclosed herein are articles of clothing having retroreflective appliqués. In some embodiments, an article of clothing includes a fabric having a first major surface and a second major surface, and a retroreflective applique attached to the first major surface of the fabric. The retroreflective applique includes a binder layer, a layer of optical elements partially embedded within the binder layer, and optionally an application layer attached to the binder layer. The optical elements include transparent microspheres and at least one reflective layer. In some embodiments, the binder layer comprises a styrenic block copolymer and at least one tackifier containing non-carbon heteroatom functional groups. In some embodiments, the application layer comprises an adhesive layer, a film layer, a fabric layer, or a nonwoven layer, wherein the application layer is attached to the first major surface of the fabric. In some embodiments, the application layer comprises a styrenic block copolymer and at least one tackifier containing non-carbon heteroatom functional groups.

Examples of articles of the invention are provided in the drawings. 2 is a cross-sectional view of one embodiment of an intermediate article of the present invention. In FIG. 2 , the intermediate article comprises a binder layer 10 , transparent microspheres 20 , a reflective layer 30 and a carrier layer 40 . The carrier layer 40 comprises a sheet layer 44 and a coating 42 of a thermoplastic polymer carrier material.

3 shows an alternative embodiment of an intermediate article of the present invention. In FIG. 3 , the intermediate article comprises a binder layer 10 , transparent microspheres 20 , a reflective layer 30 and an application layer 50 . The application layer 50 may be or include a layer of adhesive, film, cloth, or nonwoven. In some embodiments, application layer 50 is a stretchable material. In some embodiments, the fabric is selected from at least one of a cotton blend, a polyester blend, nylon, and spandex.

FIG. 4 shows the carrier layer 40 removed in the embodiment of FIG. 2 . In FIG. 4 , the article includes a binder layer 10 , transparent microspheres 20 , and a reflective layer 30 .

FIG. 5 shows the carrier layer 40 removed in the embodiment of FIG. 3 . In FIG. 5 , the article includes a binder layer 10 , transparent microspheres 20 , a reflective layer 30 and an application layer 50 . The application layer 50 may be or include a layer of adhesive, film, cloth, or nonwoven. In some embodiments, the article is wash durable.

Also disclosed herein are articles of clothing comprising the retroreflective applique of the present invention. These articles of clothing include a fabric having a first major surface and a second major surface, and a retroreflective applique attached to the first major surface of the fabric. The retroreflective applique is the retroreflective article described above. A wide variety of fabrics are suitable. In some embodiments, the fabric is a stretchable material. In some embodiments, the fabric is selected from at least one of a cotton blend, a polyester blend, nylon, and spandex.

6 shows an article of clothing of the present invention. The vest in FIG. 6 includes a retroreflective appliqué 102 . The retroreflective applique 102 may be, for example, the article of FIG. 4 or the article of FIG. 5 .

Methods of making these retroreflective articles are also disclosed herein. In some embodiments, a method of making a retroreflective article includes providing a polymeric carrier layer having a first major surface and a second major surface; providing transparent microspheres; at least partially embedding the transparent microspheres into a first major surface of the polymeric carrier layer such that the transparent microspheres at least partially protrude from the first major surface of the polymeric carrier layer to form a layer of microspheres; ; depositing one or more reflective layers on at least a portion of the first major surface of the polymeric carrier layer and the layer of microspheres; providing a binder layer on at least a portion of the reflective layer, and then optionally providing a further application layer on at least a portion of the binder layer, either the binder layer or the application layer, or both. is a rubber elastomer mixture containing a styrenic block copolymer and at least one tackifier containing non-carbon heteroatom functional groups; Finally, providing a fabric layer over at least a portion of the binder layer or the application layer. The polymer carrier layer is removed to create a wash-durable retroreflective article.

The presently disclosed retroreflective articles have either, or both, a rubber elastomeric binder layer or a rubber elastomeric application layer that enhances the durability of the retroreflective article, particularly the laundering durability of the retroreflective article. The rubber elastomeric binder layer or application layer is prepared from producing a mixture containing a styrenic block copolymer and at least one tackifier containing non-carbon heteroatom functional groups. Laundry durability is particularly important because the disclosed retroreflective articles are preferably washable. As used herein, wash durability refers to the number of times a retroreflective article can be washed using the ISO 6330 Method 6N test protocol without losing its essentially uniform appearance as defined in FIG. 7 .

Significant efforts have already been made in modifying the binder layer to make it more wash-durable, thereby improving the wash-durability of retroreflective articles. Some of these attempts have involved the use of rubber elastomeric polymers. As used herein, the term “elastomer” refers to a polymer that contains elastic properties, which give the polymer a tendency to return to its original shape after being stretched or compressed. For example, US Pat. No. 5,055,347 (Bacon) describes retroreflective articles in which retroreflective elements are embedded within an elastomeric support layer. The support layer is a reactive or curable elastomeric thermoset material, which when cured forms a strong bond.

As used herein, the terms “thermoplastic”, “non-thermoplastic” and “thermoset” refer to the properties of a material. As used herein, the term “thermoplastic material” means a material that melts or flows upon application of heat, resolidifies upon cooling, and melts or flows again upon application of heat. Thermoplastic materials undergo physical changes, such as changes in phase, rheology, or viscosity—only upon heating and cooling—but no appreciable chemical changes in the material occur. As used herein, the term “non-thermoplastic material” means a material that does not melt or flow until it reaches a temperature at which the material begins to decompose upon application of heat. As used herein, the term “thermoset material” refers to a curable material that, when heated or cured, irreversibly cures, such as becomes crosslinked. Once cured, the thermoset material will not melt or flow appreciably upon application of heat.

In some embodiments of the present invention, the rubber elastomeric binder layer is not, for example, a reactive mixture that is vulcanized or cured and is therefore referred to as a thermoplastic material rather than a thermoset material. In some embodiments, the disclosed rubber elastomeric binder layer contains at least one tackifier. In some embodiments, the at least one tackifier contains a polar (non-carbon) heteroatom functional group.

U.S. Pat. No. 6,110,558 (Billingsley) describes retroreflective articles comprising a binder layer comprising a thermoplastic copolymer comprising units containing carboxyl functional groups. In some embodiments of US Pat. No. 6,110,558 (Billingsley), the carboxyl functional groups in the thermoplastic copolymer are selected from the group consisting of acrylic acid, methacrylic acid, itaconic acid, citraconic acid, maleic acid, fumaric acid, and combinations thereof. .

In some embodiments of the present invention, the rubber elastomer is a thermoplastic copolymer that is substantially free of units of carboxyl functionality. The binder layer comprises at least one tackifier, which in some embodiments comprises non-carbon heteroatom functional groups. In some embodiments, the non-carbon heteroatom functional groups in the at least one tackifier contain carboxyl functional groups.

Generally, tackifiers are compounds used in adhesive compositions to increase tack. Tackifiers are usually low molecular weight compounds with high glass transition temperatures, with characteristic molecular weights typically less than approximately 10,000 grams/mole (g/mol). In contrast, polymer compounds commonly used in adhesives (eg, ethylene acrylic acid copolymers, rubber polymers, and acrylic block copolymers) have molecular weights of the order of about 10,000 g/mol or greater. In some embodiments, the tackifier comprises non-carbon heteroatom functional groups. In some embodiments, the heteroatom functional groups in the tackifier contain units derived from non-reactive novolac phenolic compounds. In some embodiments, the heteroatom functional groups in the tackifier contain units derived from maleic anhydride. In some embodiments, units derived from maleic anhydride are present on a thermoplastic copolymer as disclosed in US Pat. No. 6,110,558 to Billingsley, which is incorporated herein by reference in its entirety.

Examples of adhesive types include pressure sensitive adhesives, heat activated adhesives, and laminating adhesives. The pressure sensitive adhesive composition possesses properties including: (1) strong and permanent tack at room temperature, (2) adhesion under acupressure, (3) sufficient holding power on an adherend, and (4) clean removal from an adherend. sufficient cohesive strength to be Materials that have been found to function well as pressure sensitive adhesives are polymers designed and formulated to exhibit the viscoelastic properties necessary to bring about the desired balance of tack, peel adhesion and shear holding power. Achieving the right balance of characteristics is not a straightforward process. The term "pressure sensitive adhesive" refers to a composition according to the Dahlquist standard.

Heat activated adhesives are non-tacky at room temperature, but can become tacky at elevated temperatures and bond to an adherend. These adhesives usually have a glass transition temperature (Tg) or melting point (Tm) higher than room temperature. When the temperature is raised above Tg or Tm, the storage modulus usually decreases and the adhesive becomes tacky.

Laminating adhesives (sometimes referred to as contact adhesives) are adhesives designed to be sandwiched between two substrates or adherends to form a bond with these substrates to form a three-layer laminate. Laminating adhesives include hot melt adhesives, pressure sensitive adhesives, curable adhesives (ie, adhesives that are capable of undergoing a chemical reaction that cause a change in at least one property of the adhesive), and laminating by curing, cooling, drying, or other means. It may be a mixture of adhesive precursors capable of forming an adhesive. The laminating adhesive may be dispensed directly onto one or both substrates, or it may be coated between liners to form an adhesive pre-coat and subsequently laminated to one or both substrates. have. Examples of laminating hot melt adhesives include the glue stick used in hot glue guns (which is a hot melt type of adhesive that forms a bond upon cooling), casein glue, and "white glue" ( It is an aqueous dispersion that forms a bond upon drying). Examples of curable adhesives include cyanoacrylate adhesives, which cure upon exposure to air to form bonds. Examples of adhesive precursors include polymeric or oligomeric compounds such as epoxies, (meth)acrylics, polyurethanes, polysiloxanes, and polydienes.

As used herein, the term “adhesive” refers to a polymer composition useful for adhering adherends together, which can be any of the above adhesives. In some embodiments of the present invention, the rubber elastomeric binder layer or rubber elastomeric application layer comprises a laminating adhesive composition.

As used herein, the term “polymer” refers to a polymeric material that is either a homopolymer or a copolymer. As used herein, the term “homopolymer” refers to a polymeric material that is the reaction product of one type of monomer. As used herein, the term “copolymer” refers to a polymeric material that is the reaction product of at least two different types of monomers.

In the present invention, the rubber elastomeric binder layer, and optionally the application layer, comprises at least one elastomer selected from natural rubber and synthetic rubber and combinations thereof. Natural rubber (mostly contained within poly-cis-isoprene) is commonly considered to be a "non-thermoplastic hydrocarbon elastomer" that can exhibit melting temperatures that are often unmeasurable when measured using differential scanning calorimetry (DSC). ; Accordingly, in some cases, it may require special processing or compounding in order to be incorporated into the adhesive composition.

In some embodiments, the natural rubber is a polymer derived primarily from cis-1,4-polyisoprene, and ranges from a light pale crepe grade to a darker ribbed smoked sheet. may be in the range of Examples of commercially available natural rubbers that may be useful as the elastomeric component of the presently disclosed adhesive compositions include, from Akrochem, Akron, Ohio, under the trade designations "CLARIMER CV-60" (controlled viscosity rubber grade) and "SMR-5" ( ribbed smoked seat rubber grade). Natural rubber may have a molecular weight ranging from about 100,000 g/mol to about 1,000,000 g/mol. As noted above, due to their non-thermoplastic nature, many natural rubber grades may need to be poached to reduce their molecular weight to facilitate hot-melt coating, for example. This can usually be done, for example, by preprocessing in a Banbury mixer. Alternatively, US Pat. No. 5,539,033 (Bredahl) describes a twin screw extrusion compounding operation for processing natural rubber to a state where it can be incorporated into a hot-melt coatable adhesive composition.

In some embodiments, synthetic rubbers useful in the present invention include butyl rubber, synthetic polyisoprene rubber, ethylene-propylene rubber, ethylene-propylene-diene rubber, polybutadiene rubber, polyisobutylene rubber, poly(alpha-olefin) rubber. , nitrile rubber, and styrene-butadiene rubber, and, if necessary, may be processed in the manner described above for natural rubber.

In some embodiments, the rubber elastomeric adhesive composition comprises one or more block copolymers consisting essentially of only hydrogen and carbon atoms. In some embodiments, the hydrocarbon block copolymer comprises discrete blocks in one block that are substantially free of content from another block. In some embodiments, the hydrocarbon block polymer comprises one or more blocks having a measurable or even significant content attributable to other blocks; The hydrocarbon block copolymer may be referred to herein as "blocky". As used herein, the term "hydrocarbon block copolymer" includes both distinct block copolymers and block copolymers, unless otherwise specified.

In some embodiments, adhesive compositions useful in the disclosed binder layer or application layer include a block copolymer that is a styrenic block copolymer (SBC). SBCs generally include copolymers of the AB or ABA type and combinations thereof, where A represents a thermoplastic polystyrene block and B an elastomeric block such as polyisoprene, polybutadiene, poly(ethylene/butylene), poly(ethylene/propylene), or poly(isoprene/butadiene). SBC molecular weights typically range from about 100,000 grams/mole to about 1,500,000 g/mol.

Examples of useful styrene-based, or styrenic block copolymers include styrene-isoprene block copolymers, styrene-ethylene block copolymers, styrene-propylene block copolymers, styrene-ethylene-propylene block copolymers, styrene-ethylene-butyl ren block copolymers, styrene-butadiene block copolymers, styrene-isoprene-butadiene-styrene block copolymers, and combinations thereof. In some embodiments, the styrene-based block copolymer is a diblock, triblock, or higher block copolymer. In some embodiments, the styrene-based block copolymer is a styrene-isoprene diblock copolymer, a styrene-isoprene-styrene triblock copolymer, and combinations and mixtures thereof. In some embodiments, functionalized (eg, maleated) versions of any of the above block copolymers may be used. In some embodiments, the styrenic-based block copolymer is a styrenic block copolymer comprising a styrenic end block and an isoprene middle block. In some embodiments, the styrenic-based block copolymer is a styrenic block copolymer composed of a diblock of a styrenic block and an isoprene block.

SBCs useful in the present invention can be in the form of a variety of molecular structures, including linear, branched, radial, star and tapered geometries. Variations in the volume fraction of styrene in the biphasic composition lead to polystyrene domains in the shape of spheroids, cylinders, plates and co-continuous structures. In some embodiments, the weight percent of the styrene component in the one or more styrenic block copolymers is from about 5 weight percent styrene to about 50 weight percent styrene, in some embodiments from about 8 weight percent styrene to about 40 weight percent styrene; In some embodiments, it may range from about 15 weight percent styrene to 35 weight percent styrene, and in some embodiments from about 20 weight percent styrene to about 30 weight percent styrene.

Non-limiting examples of commercially available SBCs useful in the presently disclosed binder layer or application layer include styrene-isoprene block copolymers such as "KRATON D1161", "KRATON D1119" from Kraton Performance Polymers, Inc., Houston, TX. , and those commercially available as "KRATON D1117"; "VECTOR 4113" and "VECTOR 4111A" from Dexco Polymers LLP, Taipei, Taiwan; "QUINTAC 3620" from Zeon Corp., Tokyo, Japan; and "EUROPRENE SOL T 9113" from Versalis, Milan, Italy (formally Polimeri Europa S.p.A.). Non-limiting examples of commercially available SBCs useful in the disclosed binder layer also include styrene-ethylene/butylene block copolymers such as those commercially available from Kraton Performance Polymers, Inc. under the trade designation “KRATON G1657”; styrene-ethylene/propylene block copolymers such as those commercially available from Kraton Performance Polymers, Inc. under the trade designation “KRATON G1702”; styrene-butadiene block copolymers such as those commercially available from Kraton Performance Polymers, Inc. under the trade designation “KRATON D1118X”; and styrene-isoprene/butadiene block copolymers such as those commercially available from Kraton Performance Polymers, Inc. under the trade designation “KRATON D1117P”.

In some embodiments, the SBC is modified, for example, by adding one or more non-polymeric compounds such as tackifiers and/or plasticizing oils to increase tack. Any suitable tackifier that is particularly effective in combination with SBC may be used in the binder layer or application layer adhesive. In some embodiments, the tackifier and plasticizer may be used alone or in combination with each other. In some embodiments, tackifiers and plasticizers, individually or together, may be combined with the aforementioned tackifiers containing non-carbon heteroatom functional groups.

In some embodiments, non-styrenic hydrocarbon block copolymers or combinations thereof may be used with styrenic block copolymers. In some embodiments, block copolymers can include, for example, isoprene-butadiene block copolymers, ethylene-butylene block copolymers, and ethylene-propylene block copolymers.

In some embodiments, hydrocarbon block copolymers (eg, styrenic block copolymers) may include a blend of two or more such copolymers. In some embodiments, the blend of block copolymers comprises a blend of polymers that differ only in terms of overall molecular weight, molecular weight of one or more blocks, degree of branching, chemical makeup of the blocks, number of blocks, or molecular weight of block portions. In some embodiments, the blend of block copolymers has more than one such difference. In some embodiments, blends of substantially linear block copolymers and blended substantially linear triblock copolymers may be used.

In some embodiments, adhesive compositions useful in the disclosed binder layer or application layer comprise at least one tackifier, optionally at least one tackifier containing non-carbon heteroatom functional groups, and natural and synthetic rubbers and at least one elastomer selected from combinations thereof. In some embodiments, the adhesive composition may also include a hydrocarbon block copolymer, such as a styrenic block copolymer, as noted. Other ingredients may also be present in adhesive compositions useful in the present invention and are discussed later herein.

As used herein, the term “tackifier” (eg, tackifying resin) refers to increasing the glass transition temperature, decreasing the modulus, increasing the tack, or a combination of two or more thereof. means a material that is part of the adhesive as a rheology modifier for

As used herein, the term “plasticizer” (eg, plasticizing oil) refers to a rheol for lowering viscosity, reducing glass transition temperature, reducing modulus, or a combination of two or more thereof. means a material that is part of an adhesive as a lodging modifier.

As used herein, the term "acid number" means milligrams of potassium hydroxide (KOH) (mg KOH/g) required to neutralize all heteroatom functional groups present in one gram of tackifier compound, wherein Heteroatom functional groups include at least one of acidic functional groups, hydroxyl functional groups, and combinations thereof.

The present invention provides adhesives having at least one tackifier or tackifying resin containing non-carbon heteroatom functional groups useful in the disclosed binder layer or application layer. In some embodiments, the tackifier contains non-carbon heteroatom functional groups, eg, the tackifier comprises at least one of an acidic moiety, a hydroxyl moiety, and combinations thereof. In some embodiments, the tackifier containing non-carbon heteroatom functional groups has an acid number of 20 mg KOH/g to 130 mg KOH/g, in some cases 20 mg KOH/g to 90 mg KOH/g, in some cases 40 mg KOH/g to 80 mg KOH/g, in some cases 50 mg KOH/g to 70 mg KOH/g, and in some cases 55 mg KOH/g to 65 mg KOH/g. The tackifier(s) containing non-carbon heteroatom functional groups, including phenolic moieties, may have an acid number of less than 0.5 mg KOH/g, and in some cases less than 0.25 mg KOH/g.

In some embodiments, tackifiers useful in the present invention are characterized by a polarity index. In some embodiments, the polarity index of the tackifier is at least 2.5. In some embodiments, the polarity index of the tackifier is 15 or less. In some embodiments, the polarity index of the tackifier is between 2.5 and 15. As used herein, the polarity index can be calculated using the formula:

A phenolic moiety is an aromatic moiety to which at least one hydroxyl group is directly covalently bonded; The simplest phenolic moiety is derived from the compound phenol (hydroxybenzene). In some embodiments, the phenolic moiety comprises two or more aromatic rings bonded or fused together, either directly or via a linking group. In some embodiments, the phenolic moiety has two or more hydroxyl groups attached thereto. In some embodiments, one or more additional substituents, such as alkyl groups, are present on the phenolic moiety. Blends of phenolic compounds are also suitably used in the reaction leading to terpene phenolic tackifiers useful in the adhesives described herein.

Phenolic compounds include polyhydroxylated benzenes. Useful polyhydroxylated benzene compounds include dihydroxybenzene and trihydroxybenzene. The dihydroxybenzene compounds useful in the reactions herein are, in some embodiments, hydroquinone (1,4-dihydroxybenzene), catechol (1,2-dihydroxybenzene), and resorcinol ( 1,3-dihydroxybenzene). The trihydroxybenzene compounds useful in the reactions herein are, in some embodiments, phloroglucinol (1,3,5-trihydroxybenzene), hydroxyhydroquinone (1,2,4-trihydroxy benzene), and pyrogallol (1,2,3-benzenetriol). In some embodiments, polyhydroxylated adducts of naphthalene are useful in the reactions herein; Examples of such compounds include, in some embodiments, 1,2-dihydroxynaphthalene, 1,3-dihydroxynaphthalene, 1,6-dihydroxynaphthalene, 2,3-dihydroxynaphthalene, 2,7 -Dihydroxynaphthalene, etc. are included.

In some embodiments, hydroxylated and polyhydroxylated anthracene, phenanthrene, azulene, and the like are suitably used in the reaction to form one or more terpene phenolic materials useful as tackifiers in adhesives. Bisphenols, such as bisphenol A, and other compounds having a plurality of unfused aromatic rings bonded through linkages are also useful. While not wishing to be bound by theory, it is believed that it is not necessary for each aromatic ring to have a hydroxyl group if at least one aromatic ring has at least one hydroxyl group present directly bonded thereto.

Additionally, dimers, trimers, and oligomers of phenolic compounds and blends thereof are suitably employed in the reaction to form one or more terpene phenolic materials useful as tackifiers in adhesives. Such compounds include, for example, dimerized or oligomerized phenolic compounds formed through condensation with aldehydes to produce methylene or methylol ether linkages. Such compounds are widely used in industry as precursors or prepolymers for phenol-formaldehyde resins. In some embodiments, both novolak-type precursors and resol-type precursors may be useful; In some embodiments, novolac precursors are preferred. In some embodiments, the phenolic compound, or blend of phenolic compounds, is precondensed or oligomerized. To be somewhat more specific, a phenolic compound, or a combination of two or more phenolic compounds, an aldehyde in an amount selected to provide the desired level of oligomerization, and an acid used under conditions of mild heating, e.g., 50° C. to 100° C. or a basic catalyst to obtain a condensation product thereof. The oligomer thus formed has a number of reactive sites useful in subsequent steps in the formation of a tackifier useful in the adhesive composition of the present invention. In some embodiments, suitable phenolic oligomers include naturally occurring oligomeric structures such as tannic acid, humic acid, fulvic acid, and Quebracho extract.

In some embodiments, one or more additional substituents are present on one or more rings of the phenolic compound. For example, one or more alkyl, ether, halogen, amino, amido, imino, carbonyl, or other substituents, or combinations of two or more thereof, may be present as substituents bonded to the aromatic ring(s) of the phenolic compound. or as a substituent on an alkyl or alkenyl group bonded to the aromatic ring(s) of the phenolic compound. However, in many embodiments, the one or more additional substituents substantially exclude or completely exclude acidic or potentially acidic moieties. In some embodiments, the tackifier used in the adhesive is characterized as having an acid number of less than about 0.5 mg KOH/g. In some embodiments, the tackifier used in the adhesive herein is characterized as having an acid value of at least 1 mg KOH/g.

In some embodiments, phenolic compounds having more than one hydroxyl group, more than one aromatic group, and one or more additional substituents are suitably used in the reaction to form one or more tackifiers useful in the disclosed adhesives. Some examples of such compounds include 4,4′-[(1 E )-pent-1-en-4-yne-1,5-diyl]di(benzene-1,2-diol), quercetin (2- (3,4-dihydroxyphenyl)-3,5,7-trihydroxychromen-4-one), myricetin (3,5,7-trihydroxy-2-(3,4,5-) trihydroxyphenyl)chromen-4-one), theaflavin (1,8-bis(3-alpha,5,7-trihydroxy-2-alpha-chromanyl)-5H-benzocycloheptene-5 -one) and gosipol (2,2'-bis(formyl-1,6,7-trihydroxy-5-isopropyl-3-methylnaphthalene).

In some embodiments, blends of two or more of any of the phenolic compounds described herein are useful in forming tackifiers useful in the adhesives disclosed herein in various embodiments. The use of any of the above alone or in combination is not particularly limited; Rather, their selection and use are suitably tailored to produce the desired end product useful in one or more of the presently disclosed adhesive compositions.

As disclosed herein, a non-polar tackifier constitutes a compound or mixture of compounds that functions as a tackifier in the presently disclosed adhesive composition, wherein such compound or mixture of compounds is essentially free of polar groups. In some embodiments, the compound or mixture of compounds is free of polar groups. Without being bound by theory, such nonpolar tackifiers have a softening point of about 100°C to 135°C, and in some embodiments about 110°C to 120°C, and in some embodiments compatible in mixtures with styrenic block copolymers. It is believed to be

Any suitable tackifier(s) having non-carbon heteroatom functionality may be used in the present invention. Potentially suitable tackifier resins include, for example, maleic anhydride modified rosin esters (commercially available from Resinall Corp. of Severn, NC under the trade designation “RESINALL”); phenolic tackifiers (available commercially from SI Group of Skinectady, NY under the trade designations “SP25” and “SP6700”); Terpene phenol tackifier (available commercially from Yasuhara Chemicals, Hiroshima, Japan under the trade designation "T160"), from Eastman Chemicals, Kingston, Tennessee, under the trade designations "LEWISOL 28-M", "LEWISOL 29-M", "PENTALYN 702-" Maleic acid modified glycerol rosin esters and phenol modified rosin esters, including those commercially available as M", "PENTALYN 765-M", "PENTALYN 750-HV-M", "PENTALYN 770M", and "PENTALYN 755-M" Tackifiers including (but not limited to) may be included.

In some embodiments, the tackifier may be an aliphatic or aromatic material, and if multiple tackifiers are present, they may all be, in some embodiments, an aliphatic or aromatic material. In some embodiments, the tackifier or tackifiers may be hydrocarbon materials. In some embodiments, the tackifier or tackifiers are C5-derived aliphatic resins, which are obtained from unsaturated hydrocarbon feedstocks containing predominantly pentene and piperylene. Potentially suitable C5-derived aliphatic resins include those commercially available from Eastman Chemical Co. under the trade names “PICCOTAC 1020”, “PICCOTAC 1095”, “PICCOTAC 1098”, “PICCOTAC 1100”, and “PICCOTAC 1115”. In some embodiments, the tackifier or tackifiers are C9-derived aromatic resins, which are obtained from unsaturated hydrocarbon feedstock resin oils including but not limited to indene, vinyltoluene, and dicyclopentadiene. Potentially suitable resins include those commercially available from Eastman Chemical under the trade names “PICCO 2215”, “PICCO 5120”, “PICCO 5140”, and “PICCO 6100”. C5/C9-derived resins produced by mixing two feedstocks together may also be used in the present invention, including, for example, from Eastman Chemical under the trade designations "PICCOTAC 8095", "PICCOTAC 9095", "PICCOTAC 7050" There are such things as those available for purchase. In some embodiments, the adhesive composition comprises at least one tackifier containing non-carbon heteroatom functional groups, at least one styrenic block copolymer, and, optionally, at least one tack that is essentially free of non-carbon heteroatom functional groups. Includes granting agents. In some embodiments, the adhesive composition may optionally include hydrocarbon block copolymers, such as block copolymers based on styrene and isoprene.

In some embodiments, the adhesive composition comprises at least about 5 wt%, 10 wt%, 15 wt%, 20 wt%, based on the total weight of the adhesive composition, the weight percent of a tackifier containing non-carbon heteroatom functional groups; 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, or 65% by weight. In some embodiments, the tackifier containing non-carbon heteroatom functional groups is about 5 wt%, 10 wt%, 15 wt%, 20 wt%, 25 wt%, 30 wt%, based on the total weight of the adhesive composition. , 35 wt%, 40 wt%, 45 wt%, 50 wt%, 55 wt%, 60 wt%, 65 wt%, or 70 wt% or less.

All weight percentages and weight percentage ratios as used herein are based on the total weight of the components of the adhesive (when the adhesive is present on a fabric or other backing), specifically, any solvent or does not contain the presence of inert fillers (eg, mineral fillers such as calcium carbonate, titanium dioxide, talc, glass powder, silica, etc.). That is, for the purposes of all compositional calculations and ranges disclosed herein, the presence of any mineral fillers or solvents is not included.

In some embodiments, the rubber elastomer blend, such as a styrenic block copolymer blend, is about 40 wt%, 45 wt%, 50 wt%, 55 wt%, 60 wt%, 65 wt%, based on the total weight of the adhesive composition. , 70%, 75%, 80%, 85%, 90%, or 95% by weight or greater. In some embodiments, the styrenic block copolymer polymer comprises about 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75% by weight based on the total weight of the adhesive composition. It may be present in an amount up to weight percent, 80 weight percent, 85 weight percent, 95 weight percent, or 98 weight percent.

In some embodiments, the hydrocarbon block copolymer (eg, a styrenic block copolymer) is present in an amount of at least about 10%, 12%, 14%, or 16% by weight, based on the total weight of the adhesive composition. in the disclosed adhesive composition. In some embodiments, the hydrocarbon block copolymer may be present in an amount of up to about 35%, 30%, 24%, 22%, 20%, or 18% by weight, based on the total weight of the adhesive composition. . In some embodiments, the weight ratio of the total amount of hydrocarbon block copolymer to tackifier(s) (both containing and not containing non-carbon heteroatom functional groups) in the adhesive composition is at least about 25:75; It can be 30:70 or 35:65. In some embodiments, the weight ratio of the total amount of the hydrocarbon block copolymer to the tackifier (both polar and non-polar) in the adhesive composition can be up to about 50:50, 45:55, or 40:60.

In some embodiments, the adhesive composition may also include one or more additional components. For example, these additional ingredients include anti-aging agents, light and ultraviolet stabilizers (such as hindered amine light stabilizers), colorants, heat stabilizers, antimicrobial agents, fillers, crosslinking agents, and combinations thereof. but is not limited thereto.

In some embodiments, the disclosed adhesive compositions include antioxidants. While not wishing to be bound by theory, it is believed that antioxidants may be useful in preventing oxidation reactions from affecting the components of the adhesive composition. Oxidation of components can cause a variety of negative effects on the adhesive composition, including but not limited to color change, molecular weight change of polymer components, rheology change, tackiness change, release property change, and the like.

Antioxidants useful in the present invention include phenols (including hindered phenolics and bisphenolics), compounds containing mercaptan groups (including thioethers, thioesters, and mercapto-benzimidazoles), di-hydroquinolines , hydroquinones, lactates, butylated paracresols, amines, unsaturated acetals, fluorophosphonites, phosphites, and blends thereof. It will be understood that in some cases these groups are not exclusive. As an example, phenolic compounds may also have mercaptan groups.

Examples of phenolic antioxidants useful in the present invention include trade names "IRGANOX 1010", "IRGANOX 1035", "IRGANOX 1076", "IRGANOX 1098", "IRGANOX 245", " IRGANOX 3114", and those commercially available as "IRGANOX 565"; those commercially available under the trade names "ETHANOX 330", "ETHANOX 702", "ISONOX 129", and "ISONOX 132" from SI Group, Schenectady, NY; those commercially available from Solvay S.A. of Houston, TX under the trade names “CYANOX 425”, “CYANOX 2246”, and “CYANOX 1790”; those commercially available under the trade names "ULTRANOX 276", "NAUGARD BHT", "NAUGARD 76", "NAUGARD 10", "NAUGARD SP", and "NAUGARD 529" from Addivant Corporation of Danbury, Conn.; those commercially available under the trade designation "HOSTANOX 03" from Clariant International LTD. of Mutentz, Switzerland; and those commercially available from Imperial Chemical Industries of London, UK under the trade designations “TOPANOL CA”, “TOPANOL CA-SF”, and “TOPANOL 205”. Examples of mercaptan group-containing antioxidants useful in the present invention include, but are not limited to, those commercially available from BASF Corp. of Florham Park, NJ under the trade designations "IRGANOX 1726" and "IRGANOX 1520 L".

Examples of other mercaptan group-containing antioxidants useful in the present invention include those in the form of thioether antioxidants, such as those commercially available from BASF Corp. of Florham Park, NJ under the trade designations "IRGANOX PS800" and "IRGANOX PS802" Included. Other mercaptan group-containing antioxidants useful in the present invention in the form of thioester antioxidants include from Solvay SA, Houston, TX under the trade designations "CYANOX LTDP", "CYANOX STDP", "CYANOX MTDP", "CYANOX 1212", and those commercially available as "CYANOX 711".

Exemplary fluorophosphonite antioxidants useful in the present invention include those commercially available from SI Group of Schenectady, NY under the trade designation "ETHANOX 398". Examples of phosphite antioxidants useful in the present invention include those commercially available from Clariant International LTD. of Mutentz, Switzerland under the trade designation “HOSTANOX PAR 24”; those commercially available under the trade designations "WESTON619", "NAUGARD P" and "NAUGARD 524" from Addivant Corporation of Danbury, Conn.; and those commercially available from BASF Corp. of Florham Park, NJ under the trade designations “IRGAFOS 126” and “IRGAFOS 168”. Additional exemplary antioxidants useful in the present invention include trade names "IRGANOX 1330", "IRGANOX 1425", "IRGANOX 1425 WL", "IRGANOX 245 DW", "IRGANOX 5057" from BASF Corp. of Florham Park, NJ. , "IRGANOX B 1171", "IRGANOX B 215", "IRGANOX B 225", "IRGANOX B 501 W", "IRGANOX B 900", "IRGANOX E 201", "IRGANOX L 06", "IRGANOX L 101", "IRGANOX L 107", "IRGANOX L 109", "IRGANOX L 115", "IRGANOX L 118", "IRGANOX L 135", "IRGANOX L 150", "IRGANOX L 55", "IRGANOX L 57", "IRGANOX L 57", "IRGANOX L 135" L 64", "IRGANOX L 67", "IRGANOX L 74", "IRGANOX MD-1024", "IRGANOX ML-811", "IRGANOX ML-820", "IRGANOX ML-840", "IRGANOX PS 802 FL" , "IRGANOX XT 500" and "IRGASTAB FS 042".

In some embodiments, the antioxidant degrades hydroxyl or hydroperoxide groups in the adhesive composition. In some embodiments, the antioxidant degrades hydroxyl and hydroperoxide groups in the adhesive composition. In some embodiments, the amount of antioxidant used is about 0 wt%, 0.01 wt%, 0.05 wt%, 0.10 wt%, 0.20 wt%, 0.30 wt%, 0.40 wt%, 0.50 wt%, based on the total weight of the adhesive composition. %, greater than 1.00 weight percent, greater than 1.50 weight percent, or greater than 2.00 weight percent. In some embodiments, the amount of antioxidant used is about 5.00 wt%, 4.00 wt%, 3.00 wt%, 2.50 wt%, 2.00 wt%, 1.50 wt%, or 1.00 wt%, 0.80 wt%, based on the total weight of the adhesive composition. weight percent, or less than 0.50 weight percent. In some embodiments, the amount of antioxidant used can be in a range where any of the foregoing numerical values can form a lower limit or upper limit, wherein the upper limit is greater than the lower limit. For example, in some embodiments, the amount of antioxidant may range from about 0% to about 2.00% by weight based on the total weight of the adhesive composition. In some embodiments, the adhesive composition also includes at least 0.1% by weight of an antioxidant based on the total weight of the adhesive composition.

In some embodiments, the disclosed adhesive composition comprises from about 70% to about 81.5% by weight of at least one styrenic block copolymer, from about 8% to about 30% by weight of a tackifying agent having an acid value of 1 mg KOH/g or greater. agent, and about 1% by weight of an antioxidant, the weight percentages being based on the total weight of the adhesive composition. In some embodiments, the disclosed adhesive composition preferably comprises 86% by weight of a styrenic block copolymer, 13% by weight of a tackifier, and 1% by weight of an antioxidant.

In some embodiments, the adhesive composition is disposed on, for example coated on, at least a portion of one major surface of the substrate. In some embodiments, the adhesive composition may be disposed on a major surface of a substrate by disposing an adhesive precursor on the major surface and then converting the precursor to an adhesive composition. In some embodiments, this can be done by coating a precursor, which is a solvent mixture, onto a major surface, followed by removal of the solvent so that the remaining material becomes an adhesive. In some embodiments, the adhesive precursor may be cured, crosslinked, etc. as an additional step of solvent removal or in lieu of solvent removal.

In some embodiments, the adhesive composition is disposed on a substrate using a solvent-free process, such as a hot-melt coating process (eg, in a twin screw extruder, in the general manner described in U.S. Reissue Patent RE36855 (Bredahl)), wherein the adhesive The precursor is coated onto a substrate while at elevated temperature, cooled after coating or deposited, and converted into an adhesive composition. In some embodiments, these processes may be facilitated, for example, by curing, such as crosslinking, the various components of the adhesive precursor or the entire adhesive precursor, which crosslinking may be facilitated, for example, by application of an energy source, such as heat. or by using a radiation source such as exposure to actinic radiation (eg, ultraviolet light, light from a light emitting diode, also known as an LED light, etc.) and electron beam radiation.

In some embodiments, there is a continuous process in which the rubber elastomeric component of the adhesive precursor is processed (eg, in a twin screw extruder) and compounded with the other components of the adhesive precursor in the general manner described in US Reissue Patent RE36855 (Bredahl). may be used, which is incorporated herein by reference in its entirety. The thickness of the resulting adhesive composition can be any desired value, such as a value ranging from about 1 micrometer to about 200 micrometers.

In some embodiments, the disclosed adhesive compositions are hot-melt coated adhesives. Such hot-melt coated adhesives can be distinguished from adhesives prepared by other methods (e.g., solvent coating, etc.) by certain compositional indicators left in the resulting adhesive, such as the presence or absence of solvent residues, or other known indicators. have.

Example

Objects and advantages may be further illustrated by the following examples, but the specific materials and amounts thereof recited in these examples, as well as other conditions and details, should not be construed as unduly limiting the invention.

Synthesis Example S1:

Temporary glass bead carriers were prepared according to procedures as described in US Pat. No. 5,474,827 to Crandall. A poly-ethylene layer was coated onto a paper backing. The polyethylene layer was heated and glass beads having an average diameter ranging from 40 to 90 microns were cascaded and immersed into the polyethylene layer. The depth at which the glass beads were sunk was less than the average diameter of the glass beads, and a portion of the microspheres remained exposed on the surface of the polyethylene. The coated glass bead layer was vapor coated with a thin layer of aluminum metal to form an aluminum metal mirror layer.

Example 1:

86 wt % copolymer (D1119) and 13 wt % tackifier (SP25) were loaded into a twin screw extruder as pellets, together with 1 wt % antioxidant (Irganox 1520L) supplied by pipette, into a twin screw extruder at about 182° C. (360° F.) was allowed to mix in the extruder for 3 minutes. The blended formulation was then extruded onto a C420 film using a contact die with a coating thickness of approximately 0.076 millimeters. Prior to testing, the carrier liner of the C420 film was peeled off.

Example 2:

86% by weight of copolymer (D1119) and 13% by weight of tackifier (SP1077) were loaded as pellets, together with 1% by weight of antioxidant (Irganox 1520L) supplied by pipette, into a twin screw extruder at 182°C ( 360° F.) for 3 minutes in the extruder. The blended formulation was then extruded onto a C420 film using a contact die with a coating thickness of approximately 0.076 millimeters. Prior to testing, the carrier liner of the C420 film was peeled off.

Example 3:

86% by weight of copolymer (D1119) and 13% by weight of tackifier (T160) were loaded into a twin screw extruder as pellets, together with 1% by weight of antioxidant (Irganox 1520L) supplied by pipette, into a twin screw extruder at 182°C ( 360° F.) for 3 minutes in the extruder. The blended formulation was then extruded onto a C420 film using a contact die with a coating thickness of approximately 0.076 millimeters. Prior to testing, the carrier liner of the C420 film was peeled off.

Example 4:

89% by weight of copolymer (D1119) and 10% by weight of tackifier (SP1077) were loaded as pellets with 1% by weight of antioxidant (Irganox 1520L) supplied by pipette into a twin screw extruder and 182°C ( 360° F.) for 3 minutes in the extruder. The blended formulation was extruded onto a C420 film using a contact die with a coating thickness of approximately 0.076 millimeters. Prior to testing, the carrier liner of the C420 film was peeled off.

Example 5:

43% by weight of copolymer (D1119), 43% by weight of copolymer (D4411A), and 13% by weight of a tackifier (SP1077), together with 1% by weight of an antioxidant (Irganox 1520L) provided by pipette, The pellets were loaded into the twin screw extruder and allowed to mix in the extruder at 182° C. (360° F.) for 3 minutes. The blended formulation was then extruded onto a C420 film using a contact die with a coating thickness of approximately 0.076 millimeters. Prior to testing, the carrier liner of the C420 film was peeled off.

Example 6:

43 wt% copolymer (D1119), 43 wt% copolymer (D4411A), and 13 wt% tackifier (T6000), together with 1 wt% antioxidant (Irganox 1520L) provided by pipette, The pellets were loaded into the twin screw extruder and allowed to mix in the extruder at 182° C. (360° F.) for 3 minutes. The blended formulation was then extruded onto a C420 film using a contact die with a coating thickness of approximately 0.076 millimeters. Prior to testing, the carrier liner of the C420 film was peeled off.

Example 7:

43% by weight of copolymer (D1119), 43% by weight of copolymer (D4411A), and 13% by weight of a tackifier (SP25) together with 1% by weight of an antioxidant (Irganox 1520L) provided by pipette, The pellets were loaded into the twin screw extruder and allowed to mix in the extruder at 182° C. (360° F.) for 3 minutes. The blended formulation was then extruded onto a C420 film using a contact die with a coating thickness of approximately 0.076 millimeters. Prior to testing, the carrier liner of the C420 film was peeled off.

Example 8:

43% by weight of copolymer (D1119), 43% by weight of copolymer (D4411A), and 13% by weight of tackifier (T160) together with 1% by weight of antioxidant (Irganox 1520L) provided by pipette, The pellets were loaded into the twin screw extruder and allowed to mix in the extruder at 182° C. (360° F.) for 3 minutes. The blended formulation was then extruded onto a C420 film using a contact die with a coating thickness of approximately 0.076 millimeters. Prior to testing, the carrier liner of the C420 film was peeled off.

Example 9:

64% by weight of copolymer (D1119), 22% by weight of copolymer (D4411A), and 13% by weight of a tackifier (SP1077), together with 1% by weight of antioxidant (Irganox 1520L) provided by pipette, The pellets were loaded into the twin screw extruder and allowed to mix in the extruder at 182° C. (360° F.) for 3 minutes. The blended formulation was then extruded onto a C420 film using a contact die with a coating thickness of approximately 0.076 millimeters. Prior to testing, the carrier liner of the C420 film was peeled off.

Example 10:

22 wt % copolymer (D1119), 64 wt % copolymer (D4411A), and 13 wt % tackifier (SP1077) together with 1 wt % antioxidant (Irganox 1520L) provided by pipette, The pellets were loaded into the twin screw extruder and allowed to mix in the extruder at 182° C. (360° F.) for 3 minutes. The blended formulation was then extruded onto a C420 film using a contact die with a coating thickness of approximately 0.076 millimeters. Prior to testing, the carrier liner of the C420 film was peeled off.

Example 11:

22 wt % copolymer (D1119), 64 wt % copolymer (D4411A), and 13 wt % tackifier (SP25), together with 1 wt % antioxidant (Irganox 1520L) provided by pipette, The pellets were loaded into the twin screw extruder and allowed to mix in the extruder at 182° C. (360° F.) for 3 minutes. The blended formulation was then extruded onto a C420 film using a contact die with a coating thickness of approximately 0.076 millimeters. Prior to testing, the carrier liner of the C420 film was peeled off.

Example 12:

86% by weight of copolymer (D4411A) and 13% by weight of tackifier (SP25) were loaded into a twin screw extruder as pellets, together with 1% by weight of antioxidant (Irganox 1520L) supplied by pipette, into a twin screw extruder at 182°C ( 360° F.) for 3 minutes in the extruder. The blended formulation was then extruded onto a C420 film using a contact die with a coating thickness of approximately 0.076 millimeters. Prior to testing, the carrier liner of the C420 film was peeled off.

Example 13:

22 wt% copolymer (D1119), 64 wt% copolymer (D4411A), and 13 wt% tackifier (Resinall 476) together with 1 wt% antioxidant (Irganox 1520L) provided by pipette , loaded into the twin screw extruder as pellets and allowed to mix in the extruder at 182° C. (360° F.) for 3 minutes. The blended formulation was then extruded onto a C420 film using a contact die with a coating thickness of approximately 0.076 millimeters. Prior to testing, the carrier liner of the C420 film was peeled off.

Example 14:

86% by weight of copolymer (D1119) and 13% by weight of tackifier (SP25) were loaded into a twin screw extruder as pellets, together with 1% by weight of antioxidant (Irganox 1520L) supplied by pipette, into a twin screw extruder at 182°C ( 360° F.) for 3 minutes in the extruder. The blended formulation was then extruded onto PET fabric using a contact die with a coating thickness of approximately 0.076 millimeters. The sheet of vapor coated glass bead layer from Synthesis Example S1 was then subjected to a Hix N-800 clamshell laminator at a pressure of 206,843 Newtons per square meter (30 psi) and a temperature of 275°F (135°C) for 10 seconds. was used for hot lamination on the adhesive. Prior to testing, the carrier liner from Synthesis Example S1 was peeled off.

Example 15:

70 wt % copolymer (D1119) and 30 wt % tackifier (Resinall 476) were loaded as pellets into a twin screw extruder and allowed to mix in the extruder at 182° C. (360° F.) for 3 minutes. The blended formulation was then extruded onto PET fabric using a contact die with a coating thickness of approximately 0.076 millimeters. The sheet of vapor coated glass bead layer from Synthesis Example S1 was then glued using a Hix N-800 clamshell laminator at a pressure of 206,843 Newtons per square meter (30 psi) and a temperature of 275°F (135°C) for 10 seconds. It was laminated on the high temperature. Prior to testing, the carrier liner from Synthesis Example S1 was peeled off.

Comparative Example C1:

81.5 wt% copolymer (D1119), 12.5 wt% tackifier (K100), and 5 wt% tackifier (SP1077) together with 1 wt% antioxidant (Irganox 1520L) provided by pipette , loaded into the twin screw extruder as pellets and allowed to mix in the extruder at 182° C. (360° F.) for 3 minutes. The blended formulation was then extruded onto a C420 film using a contact die with a coating thickness of approximately 0.076 millimeters. Prior to testing, the carrier liner of the C420 film was peeled off.

Comparative Example C2:

81.5 wt % copolymer (D1119), 12.5 wt % tackifier (K100), and 5 wt % tackifier (SP1068) together with 1 wt % antioxidant (Irganox 1520L) provided by pipette , loaded into the twin screw extruder as pellets and allowed to mix in the extruder at 182° C. (360° F.) for 3 minutes. The blended formulation was then extruded onto a C420 film using a contact die with a coating thickness of approximately 0.076 millimeters. Prior to testing, the carrier liner of the C420 film was peeled off.

Comparative Example C3:

81.5 wt % copolymer (D1119), 12.5 wt % tackifier (K100), and 5 wt % tackifier (SP6700) together with 1 wt % antioxidant (Irganox 1520L) provided by pipette , loaded into the twin screw extruder as pellets and allowed to mix in the extruder at 182° C. (360° F.) for 3 minutes. The blended formulation was then extruded onto a C420 film using a contact die with a coating thickness of approximately 0.076 millimeters. Prior to testing, the carrier liner of the C420 film was peeled off.

Comparative Example C4:

81.5 wt % copolymer (D1119), 12.5 wt % tackifier (K100), and 5 wt % tackifier (SP25) together with 1 wt % antioxidant (Irganox 1520L) provided by pipette , loaded into the twin screw extruder as pellets and allowed to mix in the extruder at 182° C. (360° F.) for 3 minutes. The blended formulation was then extruded onto a C420 film using a contact die with a coating thickness of approximately 0.076 millimeters. Prior to testing, the carrier liner of the C420 film was peeled off.

Comparative Example C5:

86% by weight of copolymer (D1119) and 13% by weight of tackifier (K100) were loaded into a twin screw extruder as pellets, together with 1% by weight of antioxidant (Irganox 1520L) supplied by pipette, into a twin screw extruder at 182°C ( 360° F.) for 3 minutes in the extruder. The blended formulation was then extruded onto a C420 film using a contact die with a coating thickness of approximately 0.076 millimeters. Prior to testing, the carrier liner of the C420 film was peeled off.

Comparative Example C6:

61 wt% copolymer (D1119), 20.5 wt% copolymer (D4411A), 12.5 wt% tackifier (K100), and 5 wt% tackifier (SP1077), 1 wt% pipetted % antioxidant (Irganox 1520L), loaded as pellets into the twin screw extruder and allowed to mix in the extruder at 182° C. (360° F.) for 3 minutes. The blended formulation was then extruded onto a C420 film using a contact die with a coating thickness of approximately 0.076 millimeters. Prior to testing, the carrier liner of the C420 film was peeled off.

Comparative Example C7:

92% by weight of copolymer (D1119) and 7% by weight of tackifier (SP25), together with 1% by weight of antioxidant (Irganox 1520L) supplied by pipette, were loaded as pellets into a twin screw extruder, 182°C ( 360° F.) for 3 minutes in the extruder. The blended formulation was then extruded onto a C420 film using a contact die with a coating thickness of approximately 0.076 millimeters. Prior to testing, the carrier liner of the C420 film was peeled off.

Comparative Example C8:

86% by weight of copolymer (D1119), 9% by weight of tackifier (SP25) and 4% by weight of mineral oil, together with 1% by weight of antioxidant (Irganox 1520L) provided by pipette, into a twin screw extruder as pellets loaded and allowed to mix in the extruder at 182° C. (360° F.) for 3 minutes. The blended formulation was then extruded onto a C420 film using a contact die with a coating thickness of approximately 0.076 millimeters. Prior to testing, the carrier liner of the C420 film was peeled off.

Comparative Example C9:

43% by weight of copolymer (D1119), 43% by weight of copolymer (D4411A) and 13% by weight of a tackifier (Escorez 5380) together with 1% by weight of an antioxidant (Irganox 1520L) provided by pipette, The pellets were loaded into the twin screw extruder and allowed to mix in the extruder at 182° C. (360° F.) for 3 minutes. The blended formulation was then extruded onto a C420 film using a contact die with a coating thickness of approximately 0.076 millimeters. Prior to testing, the carrier liner of the C420 film was peeled off.

Comparative Example C10:

43% by weight of copolymer (D1119), 43% by weight of copolymer (D4411A) and 13% by weight of a tackifier (Escorez 5690) together with 1% by weight of an antioxidant (Irganox 1520L) provided by pipette, The pellets were loaded into the twin screw extruder and allowed to mix in the extruder at 182° C. (360° F.) for 3 minutes. The blended formulation was then extruded onto a C420 film using a contact die with a coating thickness of approximately 0.076 millimeters. Prior to testing, the carrier liner of the C420 film was peeled off.

Comparative Example C11:

43% by weight of copolymer (D1119), 43% by weight of copolymer (D4411A) and 13% by weight of a tackifier (Arkon M90) together with 1% by weight of antioxidant (Irganox 1520L) provided by pipette, The pellets were loaded into the twin screw extruder and allowed to mix in the extruder at 182° C. (360° F.) for 3 minutes. The blended formulation was then extruded onto a C420 film using a contact die with a coating thickness of approximately 0.076 millimeters. Prior to testing, the carrier liner of the C420 film was peeled off.

Comparative Example C12:

43 wt% copolymer (D1119), 43 wt% copolymer (D4411A), and 13 wt% tackifier (P90HS), together with 1 wt% antioxidant (Irganox 1520L) provided by pipette, The pellets were loaded into the twin screw extruder and allowed to mix in the extruder at 182° C. (360° F.) for 3 minutes. The blended formulation was then extruded onto a C420 film using a contact die with a coating thickness of approximately 0.076 millimeters. Prior to testing, the carrier liner of the C420 film was peeled off.

Comparative Example C13:

43% by weight of copolymer (D1119), 43% by weight of copolymer (D4411A), and 13% by weight of tackifier (K100) together with 1% by weight of antioxidant (Irganox 1520L) provided by pipette, The pellets were loaded into the twin screw extruder and allowed to mix in the extruder at 182° C. (360° F.) for 3 minutes. The blended formulation was then extruded onto a C420 film using a contact die with a coating thickness of approximately 0.076 millimeters. Prior to testing, the carrier liner of the C420 film was peeled off.

Comparative Example C14:

22% by weight of copolymer (D1119), 64% by weight of copolymer (D4411A) and 13% by weight of a tackifier (Escorez 5340) together with 1% by weight of antioxidant (Irganox 1520L) provided by pipette, The pellets were loaded into the twin screw extruder and allowed to mix in the extruder at 182° C. (360° F.) for 3 minutes. The blended formulation was then extruded onto a C420 film using a contact die with a coating thickness of approximately 0.076 millimeters. Prior to testing, the carrier liner of the C420 film was peeled off.

Comparative Example C15:

22% by weight of copolymer (D1119), 64% by weight of copolymer (D4411A) and 13% by weight of a tackifier (Escorez 5637) together with 1% by weight of antioxidant (Irganox 1520L) provided by pipette, The pellets were loaded into the twin screw extruder and allowed to mix in the extruder at 182° C. (360° F.) for 3 minutes. The blended formulation was then extruded onto a C420 film using a contact die with a coating thickness of approximately 0.076 millimeters. Prior to testing, the carrier liner of the C420 film was peeled off.

Comparative Example C16:

22% by weight of copolymer (D1119), 64% by weight of copolymer (D4411A) and 13% by weight of a tackifier (Arkon M135) together with 1% by weight of antioxidant (Irganox 1520L) provided by pipette, The pellets were loaded into the twin screw extruder and allowed to mix in the extruder at 182° C. (360° F.) for 3 minutes. The blended formulation was then extruded onto a C420 film using a contact die with a coating thickness of approximately 0.076 millimeters. Prior to testing, the carrier liner of the C420 film was peeled off.

Comparative Example C17:

22% by weight of copolymer (D1119), 64% by weight of copolymer (D4411A), and 13% by weight of a tackifier (P140) together with 1% by weight of antioxidant (Irganox 1520L) provided by pipette, The pellets were loaded into the twin screw extruder and allowed to mix in the extruder at 182° C. (360° F.) for 3 minutes. The blended formulation was then extruded onto a C420 film using a contact die with a coating thickness of approximately 0.076 millimeters. Prior to testing, the carrier liner of the C420 film was peeled off.

Polarity index calculation:

The polarity index for each sample was calculated as follows:

Washing Durability Test:

Polyester/cotton 85/15 orange cloth ^{weighing 270 g/m 2} using a Hix N-800 clamshell laminator at 275,790 newtons/square meter (40 pounds/square inch), 135°C (275°F) for 20 seconds. Test samples of the articles of Examples 1-15 and Comparative Examples C1-C17 were prepared by laminating onto a piece. Test samples of the articles of Examples 14 and 15 were prepared by sewing an appliqué of the fabric article onto a piece of polyester/cotton 85/15 fluorescent orange fabric weighing 270 grams per square meter. The sample was then washed according to method 6N of ISO 6330 for 25 cycles. The samples were then visually observed after testing, and a designation of “yes” or “no” for “good appearance” was given to each sample. As shown in FIG. 7 , a designation of “Yes” was given to “Good Appearance” if the sample was still on the orange cloth, showed a uniform appearance, and had no flakes. The results are shown in Table 1. Examples 1 to 15 show good appearance after washing.

[Table 1]

Claims (14)

An adhesive composition comprising:
styrenic block copolymer; and
at least one tackifier
including,
said at least one tackifier contains a non-carbon heteroatom functional group;
wherein the adhesive composition is wash-durable when bonded to a substrate. The adhesive composition of claim 1 , wherein the at least one tackifier containing a non-carbon heteroatom functional group has an acid number of at least 1 mg KOH/g. The adhesive composition of claim 1 , wherein the adhesive composition is a laminating adhesive. The adhesive composition of claim 1 , wherein the adhesive composition is a heat activated adhesive. The adhesive composition according to claim 2, wherein the polarity index of the tackifier is 2.5 or more. The adhesive composition of claim 2, wherein the composition has a polarity index of 2.5 to 15. The adhesive composition of claim 1 , wherein the styrenic block copolymer comprises a styrenic end block and an isoprene intermediate block. The adhesive composition of claim 1, wherein the styrenic block copolymer comprises a diblock of a styrenic block and an isoprene block. The adhesive composition of claim 1 , wherein the total weight percent of all tackifiers in the adhesive composition is at least 5 weight percent based on the total weight of the adhesive composition. 10. The adhesive composition according to any one of claims 1 to 9, further comprising at least 0.1% by weight of an antioxidant based on the total weight of the adhesive composition. 11. An article comprising the adhesive composition of any one of claims 1-10 adhered to a laminating substrate. The article of claim 11 , wherein the laminating substrate is selected from at least one of a layer of another adhesive, a film layer, a fabric layer, or a non-woven layer. The article of claim 11 , further comprising a retroreflective applique disposed on the side of the adhesive composition opposite the laminating substrate. The article of claim 13 , wherein the retroreflective applique is disposed on an article of clothing.

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